Suchergebnisse - (Subject:"Otorhinolaryngologic Diseases")

PubPharm (2)

1

Analysis of Rotterdam Study cohorts confirms a previously identified RIPOR2 in-frame deletion as a prevalent genetic factor in phenotypically variable adult-onset hearing loss (DFNA21) in the Netherlands

enthalten in: Journal of medical genetics | 2023

von Velde, H. | Homans, N. | Goedegebure, A. | +3

2

TMPRSS3 expression is limited in spiral ganglion neurons : implication for successful cochlear implantation

enthalten in: Journal of medical genetics | 2022

von Chen, Y. | Cabrera, E. | Tucker, B. | +5

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